Статті в журналах з теми "Stereoselective reaction"
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Misra, Anup Kumar, Arin Gucchait, and Monalisa Kundu. "Synthesis of Pentasaccharide Repeating Unit Corresponding to the Cell Wall O-Polysaccharide of Salmonella enterica O55 Strain Containing a Rare Sugar 3-Acetamido-3-deoxy-d-fucose." Synthesis 53, no. 19 (June 24, 2021): 3613–20. http://dx.doi.org/10.1055/s-0037-1610777.
Повний текст джерелаRossi, Sergio, Tiziana Benincori, Laura Maria Raimondi, and Maurizio Benaglia. "3,3′-Bithiophene-Based Chiral Bisphosphine Oxides as Organocatalysts in Silicon-Derived Lewis Acid Mediated Reactions." Synlett 31, no. 06 (January 7, 2020): 535–46. http://dx.doi.org/10.1055/s-0039-1690777.
Повний текст джерелаKlegraf, Ellen, and Horst Kunz. "Stereoselective Synthesis of 3-Substituted and 3,4-Disubstituted Piperidine und Piperidin-2-one Derivatives." Zeitschrift für Naturforschung B 67, no. 4 (April 1, 2012): 389–405. http://dx.doi.org/10.1515/znb-2012-0413.
Повний текст джерелаWoo, Simon, Masood Parvez, and Brian A. Keay. "Regio- and stereoselective ring openings of unsymmetrical oxatricyclo adducts." Canadian Journal of Chemistry 75, no. 6 (June 1, 1997): 665–80. http://dx.doi.org/10.1139/v97-081.
Повний текст джерелаPenumati, Nageshwar Rao, та Nagaiah Kommu. "Stereoselective Synthesis of (+)-α-Conhydrine from R-(+)-Glyceraldehyde". Organic Chemistry International 2014 (20 жовтня 2014): 1–7. http://dx.doi.org/10.1155/2014/982716.
Повний текст джерелаSchultz, Jeremy F., Bing Yang, and Nan Jiang. "Direct observation of the geometric isomer selectivity of a reaction controlled via adsorbed bromine." Nanoscale 12, no. 4 (2020): 2726–31. http://dx.doi.org/10.1039/c9nr09857g.
Повний текст джерелаLiu, Yuxiao, Yongming Deng, Peter Y. Zavalij, Renhua Liu та Michael P. Doyle. "An efficient route to highly enantioenriched tetrahydroazulenes and β-tetralones by desymmetrization reactions of δ,δ-diaryldiazoaceto-acetates". Chemical Communications 51, № 3 (2015): 565–68. http://dx.doi.org/10.1039/c4cc08255a.
Повний текст джерелаRoss, Günther, та Ivar Ugi. "Stereoselective syntheses of α-amino acid and peptide derivatives by the U-4CR of 5-desoxy-5-thio-D-xylopyranosylamine". Canadian Journal of Chemistry 79, № 12 (1 грудня 2001): 1934–39. http://dx.doi.org/10.1139/v01-186.
Повний текст джерелаCantin, Michel, Yao-Chang Xu, and Pierre Deslongchamps. "Stereocontrolled construction of A.B.C.[6.6.6] tricycle via transannular Diels–Alder reaction of 14-membered triene macrocycle." Canadian Journal of Chemistry 68, no. 12 (December 1, 1990): 2144–52. http://dx.doi.org/10.1139/v90-329.
Повний текст джерелаSugita, Kazuyuki, Motoi Kuwabara, Ami Matsuo, Shogo Kamo, and Akinobu Matsuzawa. "Stereoselective Convergent Synthesis of Carbon Skeleton of Cotylenin A Aglycone." Synthesis 53, no. 12 (February 1, 2021): 2092–102. http://dx.doi.org/10.1055/s-0040-1706684.
Повний текст джерелаYang, Yang. "Building polyfunctional piperidines: a stereoselective strategy of a three-component Mannich reaction inspired by biosynthesis and applications in the synthesis of natural alkaloids (+)-241D; (−)-241D; isosolenopsin A and (−)-epimyrtine." RSC Advances 5, no. 24 (2015): 18894–908. http://dx.doi.org/10.1039/c4ra14418j.
Повний текст джерелаYajima, Tomoko, Eriko Yoshida та Masako Hamano. "Diastereoselective radical addition to γ-alkyl-α-methylene-γ-butyrolactams and the synthesis of a chiral pyroglutamic acid derivative". Beilstein Journal of Organic Chemistry 9 (17 липня 2013): 1432–36. http://dx.doi.org/10.3762/bjoc.9.161.
Повний текст джерелаFischer, Róbert, Ondrej Záborský, Radka Štadániová, Jana Doháňošová, and Ján Moncol. "Synthesis of Isoxazolidinyl Epoxides by Oxone Treatment of 2,3-Dihydroisoxazoles in Acetone–Water Solution: A New Stereoselective Approach to Hydroxy-Substituted Isoxazolidines." Synthesis 49, no. 22 (September 27, 2017): 4942–54. http://dx.doi.org/10.1055/s-0036-1590924.
Повний текст джерелаShindo, M., and K. Yaji. "Scandium-Catalyzed Stereoselective Nazarov Reaction." Synfacts 2009, no. 12 (November 20, 2009): 1358. http://dx.doi.org/10.1055/s-0029-1218236.
Повний текст джерелаRiant, O., O. Chuzel, J. Deschamps, and C. Chausteur. "Stereoselective Tandem Reductive Aldol Reaction." Synfacts 2007, no. 3 (March 2007): 0313. http://dx.doi.org/10.1055/s-2007-968183.
Повний текст джерелаGangadhar, Pamarthi, Sayini Ramakrishna, Ponneri Venkateswarlu, and Pabbaraja Srihari. "Stereoselective total synthesis and structural revision of the diacetylenic diol natural products strongylodiols H and I." Beilstein Journal of Organic Chemistry 14 (September 4, 2018): 2313–20. http://dx.doi.org/10.3762/bjoc.14.206.
Повний текст джерелаJanzen, Alexander F., and Meehae Jang. "Isomerization, fluorine exchange, and stereoselective synthesis of cis- and trans-F2TePh3Cl: application of the coordination model of reaction mechanisms." Canadian Journal of Chemistry 67, no. 1 (January 1, 1989): 71–75. http://dx.doi.org/10.1139/v89-012.
Повний текст джерелаEscalante, Carlos H., Eder I. Martínez-Mora, Carlos Espinoza-Hicks, Alejandro A. Camacho-Dávila, Fernando R. Ramos-Morales, Francisco Delgado, and Joaquín Tamariz. "Highly selective Diels–Alder and Heck arylation reactions in a divergent synthesis of isoindolo- and pyrrolo-fused polycyclic indoles from 2-formylpyrrole." Beilstein Journal of Organic Chemistry 16 (June 17, 2020): 1320–34. http://dx.doi.org/10.3762/bjoc.16.113.
Повний текст джерелаPereira, Ana Margarida, Honorina Cidade, and Maria Elizabeth Tiritan. "Stereoselective Synthesis of Flavonoids: A Brief Overview." Molecules 28, no. 1 (January 3, 2023): 426. http://dx.doi.org/10.3390/molecules28010426.
Повний текст джерелаFeng, Xiujuan, Haixia Zhang, Wenbo Lu, Yoshinori Yamamoto, Abdulrahman Almansour, Natarajan Arumugam, Raju Kumar, and Ming Bao. "Stereoselective Synthesis of Vinyl Iodides through Copper(I)-Catalyzed Finkelstein-Type Halide-Exchange Reaction." Synthesis 49, no. 12 (April 11, 2017): 2727–32. http://dx.doi.org/10.1055/s-0036-1588988.
Повний текст джерелаSmetanin, N. V., S. A. Varenichenko, A. V. Mazepa, O. K. Farat, A. V. Kharchenko, and V. I. Markov. "Atom-economic Michael reaction between hydroacridines and arylmaleimides without catalyst/additive." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 5 (October 2022): 102–9. http://dx.doi.org/10.32434/0321-4095-2022-144-5-102-109.
Повний текст джерелаDarvesh, Sultan, Andrew S. Grant, David I. Magee, and Zdenek Valenta. "An approach to the synthesis of bruceantin. The synthesis of a tetracyclic intermediate." Canadian Journal of Chemistry 67, no. 12 (December 1, 1989): 2237–40. http://dx.doi.org/10.1139/v89-348.
Повний текст джерелаKarak, Milandip, Luiz C. A. Barbosa, Jaime A. M. Acosta, Ariel M. Sarotti, and John Boukouvalas. "Thermodynamically driven, syn-selective vinylogous aldol reaction of tetronamides." Organic & Biomolecular Chemistry 14, no. 21 (2016): 4897–907. http://dx.doi.org/10.1039/c6ob00895j.
Повний текст джерелаClark, J. Stephen, and Michael Popadynec. "Stereoselective Synthesis of the I–L Fragment of the Pacific Ciguatoxins." Toxins 12, no. 12 (November 24, 2020): 740. http://dx.doi.org/10.3390/toxins12120740.
Повний текст джерелаTarui, Atsushi, Yukiko Karuo, Kazuyuki Sato, Kentaro Kawai та Masaaki Omote. "Stereoselective Synthesis of Multisubstituted α-fluoro-β-lactams". Current Organic Chemistry 24, № 18 (18 листопада 2020): 2169–80. http://dx.doi.org/10.2174/1385272824666200221114707.
Повний текст джерелаSoorukram, Darunee, Manat Pohmakotr, Chutima Kuhakarn, and Vichai Reutrakul. "Stereoselective Synthesis of Tetrahydrofuran Lignans." Synthesis 50, no. 24 (October 2, 2018): 4746–64. http://dx.doi.org/10.1055/s-0037-1610289.
Повний текст джерелаSingh, Nidhi, and Jaya Pandey. "Advances in Henry Reaction: A Versatile Method in Organic Synthesis." Mini-Reviews in Organic Chemistry 17, no. 3 (April 28, 2020): 297–308. http://dx.doi.org/10.2174/1570193x16666190214150144.
Повний текст джерелаGualandi, Andrea, Luca Mengozzi, and Pier Cozzi. "Stereoselective SN1-Type Reaction of Enols and Enolates." Synthesis 49, no. 15 (June 13, 2017): 3433–43. http://dx.doi.org/10.1055/s-0036-1588871.
Повний текст джерелаBaikadi, Karunakar, Anil Talakokkula, and A. Narsaiah. "Stereoselective Total Synthesis of Macrolide Sch-725674 and C-7-epi-Sch-725674." SynOpen 03, no. 01 (January 2019): 26–35. http://dx.doi.org/10.1055/s-0037-1611665.
Повний текст джерелаLiu, Yingchun, Ted S. Sorensen, and Fang Sun. "Stereoselective 1,3-debromination reactions." Canadian Journal of Chemistry 71, no. 2 (February 1, 1993): 258–62. http://dx.doi.org/10.1139/v93-037.
Повний текст джерелаSoto, Martín, Irene Sanz-Machín, Humberto Rodríguez-Solla, and Vicente Gotor-Fernández. "Chemoenzymatic Stereoselective Synthesis of trans-Flavan-4-ols via Lipase-Catalyzed Kinetic Resolutions." Catalysts 11, no. 11 (October 27, 2021): 1296. http://dx.doi.org/10.3390/catal11111296.
Повний текст джерелаKhrimyan, Ashot P., Oganes A. Gharibyan, Ludvík Streinz, Zdeněk Wimmer, Miroslav Romaňuk та Shaliko O. Badanyan. "The hydroalumination-iodination of enyne α-alcohols: Synthesis of 3-methyl-2,4-alkadien-1-ols". Collection of Czechoslovak Chemical Communications 54, № 12 (1989): 3284–93. http://dx.doi.org/10.1135/cccc19893284.
Повний текст джерелаMarin, Lucile, Soufyan Jerhaoui, Emilie Kolodziej, Régis Guillot, Vincent Gandon, Françoise Colobert, Emmanuelle Schulz, Joanna Wencel‐Delord, and David Lebœuf. "Sulfoxide‐Controlled Stereoselective Aza‐Piancatelli Reaction." Advanced Synthesis & Catalysis 363, no. 17 (July 29, 2021): 4277–82. http://dx.doi.org/10.1002/adsc.202100848.
Повний текст джерелаBaba, A., S. Babu, M. Yasuda, Y. Okabe, and I. Shibata. "Stereoselective Reformatsky Reaction of Indium Enolates." Synfacts 2006, no. 9 (September 2006): 0930. http://dx.doi.org/10.1055/s-2006-949268.
Повний текст джерелаRama Rao, K., T. N. Srinivasan, and N. Bhanumathi. "A stereoselective biocatalytic diels-alder reaction." Tetrahedron Letters 31, no. 41 (January 1990): 5959–60. http://dx.doi.org/10.1016/s0040-4039(00)98004-3.
Повний текст джерелаByk, G., and E. Kabha. "A Solid-Supported Stereoselective Multicomponent Reaction." Synfacts 2006, no. 7 (June 2006): 0739. http://dx.doi.org/10.1055/s-2006-941902.
Повний текст джерелаBauer, Adriano, and Nuno Maulide. "A Stereoselective Reductive Hosomi–Sakurai Reaction." Organic Letters 20, no. 5 (February 22, 2018): 1461–64. http://dx.doi.org/10.1021/acs.orglett.8b00276.
Повний текст джерелаKapa, Prasad, Chen Kau-Ming, Repic Oljan, and Hardtmann E. Goetz. "Stereoselective aldol reaction with chiral acetates." Tetrahedron: Asymmetry 1, no. 10 (January 1990): 703–6. http://dx.doi.org/10.1016/s0957-4166(00)82378-2.
Повний текст джерелаRoy, Tamal, Myungjo J. Kim, Yang Yang, Suyeon Kim, Gyumin Kang, Xinyi Ren, Anders Kadziola, Hee-Yoon Lee, Mu-Hyun Baik, and Ji-Woong Lee. "Carbon Dioxide-Catalyzed Stereoselective Cyanation Reaction." ACS Catalysis 9, no. 7 (May 2019): 6006–11. http://dx.doi.org/10.1021/acscatal.9b01087.
Повний текст джерелаSANO, Shigeki. "Development of Highly Stereoselective Reactions Utilizing Heteroatoms : New Approach to the Stereoselective Horner-Wadsworth-Emmons Reaction." YAKUGAKU ZASSHI 120, no. 5 (2000): 432–44. http://dx.doi.org/10.1248/yakushi1947.120.5_432.
Повний текст джерелаGrigg, Ronald, Suren Husinec, and Vladimir Savic. "Stereoselective cyclo-addition reactions of azomethine ylides catalysed by in situ generated Ag(I)/bisphosphine complexes." Journal of the Serbian Chemical Society 75, no. 1 (2010): 1–9. http://dx.doi.org/10.2298/jsc1001001g.
Повний текст джерелаVarga, Eszter, László Tamás Mika, Antal Csámpai, Tamás Holczbauer, György Kardos, and Tibor Soós. "Mechanistic investigations of a bifunctional squaramide organocatalyst in asymmetric Michael reaction and observation of stereoselective retro-Michael reaction." RSC Advances 5, no. 115 (2015): 95079–86. http://dx.doi.org/10.1039/c5ra19593d.
Повний текст джерелаAitouna, Abdelhak Ouled, Ali Barhoumi, and Abdellah Zeroual. "A Mechanism Study and an Investigation of the Reason for the Stereoselectivity in the [4+2] Cycloaddition Reaction between Cyclopentadiene and Gem-substituted Ethylene Electrophiles." Scientiae Radices 2, no. 3 (July 27, 2023): 217–28. http://dx.doi.org/10.58332/scirad2023v2i3a01.
Повний текст джерелаBusfield, WK, DI Grice, ID Jenkins, and SH Thang. "Reaction of t-Butoxy Radicals With Cyclic Alkenes Studied by the Nitroxide Radical-Trapping Technique." Australian Journal of Chemistry 44, no. 10 (1991): 1407. http://dx.doi.org/10.1071/ch9911407.
Повний текст джерелаMinko, Yury, Morgane Pasco, Helena Chechik, and Ilan Marek. "Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides." Beilstein Journal of Organic Chemistry 9 (March 13, 2013): 526–32. http://dx.doi.org/10.3762/bjoc.9.57.
Повний текст джерелаSingh, Surinderjit, M. PS Ishar, Gajendra Singh, and Rajinder Singh. "Efficient, microwave-assisted intramolecular 1,3-dipolar cycloadditions of oximes and N-methylnitrones derived from o-alkenylmethoxy-acetophenones." Canadian Journal of Chemistry 83, no. 3 (March 1, 2005): 260–65. http://dx.doi.org/10.1139/v05-049.
Повний текст джерелаGhorai, Manas K., Subhomoy Das, Kalpataru Das, and Amit Kumar. "Stereoselective synthesis of activated 2-arylazetidines via imino-aldol reaction." Organic & Biomolecular Chemistry 13, no. 34 (2015): 9042–49. http://dx.doi.org/10.1039/c5ob01140j.
Повний текст джерелаVereshchagin, Anatoly N., Taigib M. Iliyasov, Kirill A. Karpenko, Radmir N. Akchurin, and Mikhail E. Minyaev. "Tetrahydropyridines’ Stereoselective Formation, How Lockdown Assisted in the Identification of the Features of Its Mechanism." Molecules 27, no. 14 (July 7, 2022): 4367. http://dx.doi.org/10.3390/molecules27144367.
Повний текст джерелаElinson, M. N., A. N. Vereshchagin, R. F. Nasybullin, S. I. Bobrovsky, A. I. Ilovaisky, V. M. Merkulova, I. S. Bushmarinov, and M. P. Egorov. "General approach to a spiro indole-3,1′-naphthalene tetracyclic system: stereoselective pseudo four-component reaction of isatins and cyclic ketones with two molecules of malononitrile." RSC Advances 5, no. 62 (2015): 50421–24. http://dx.doi.org/10.1039/c5ra03452c.
Повний текст джерелаAndreev, Mikhail V., Vladimir A. Potapov, Maxim V. Musalov, and Lyudmila I. Larina. "A New Family of Vinyl Selenocyanates with the Amide Function Based on the Reaction of Potassium Selenocyanate with 3-Trimethylsilyl-2-Propynamides." Catalysts 13, no. 9 (August 30, 2023): 1257. http://dx.doi.org/10.3390/catal13091257.
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